(Q34630270)

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The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes.

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3 February 2020

The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes (English)

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3 February 2020

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3 February 2020

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C A Stratakis

1

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3 February 2020

M A Tichomirowa

2

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3 February 2020

S Boikos

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3 February 2020

M F Azevedo

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3 February 2020

M Lodish

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3 February 2020

M Martari

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3 February 2020

S Verma

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3 February 2020

M Raygada

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3 February 2020

M F Keil

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3 February 2020

J Papademetriou

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3 February 2020

L Drori-Herishanu

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3 February 2020

A Horvath

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3 February 2020

K M Tsang

14

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3 February 2020

M Nesterova

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3 February 2020

S Franklin

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3 February 2020

J-F Vanbellinghen

17

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3 February 2020

V Bours

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3 February 2020

R Salvatori

19

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3 February 2020

A Beckers

20

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3 February 2020

publication date

1 November 2010

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3 February 2020

Clinical Genetics

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3 February 2020

78

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3 February 2020

5

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3 February 2020

457-463

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3 February 2020

Familial pituitary adenomas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

The pathogenesis of pituitary tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

An Intronic mutation is associated with prolactinoma in a young boy, decreased penetrance in his large family, and variable effects on MEN1 mRNA and protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

Mutations in regulatory subunit type 1A of cyclic adenosine 5'-monophosphate-dependent protein kinase (PRKAR1A): phenotype analysis in 353 patients and 80 different genotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

Update on the treatment of pituitary adenomas: familial and genetic considerations

1 reference

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7 July 2018

Rare germline mutations in cyclin-dependent kinase inhibitor genes in multiple endocrine neoplasia type 1 and related states

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

Pituitary tumors in childhood: update of diagnosis, treatment and molecular genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

SplicePort--an interactive splice-site analysis tool

1 reference

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7 July 2018

A possible new syndrome with growth-hormone secreting pituitary adenoma, colonic polyposis, lipomatosis, lentigines and renal carcinoma in association with familial testicular germ cell malignancy: A case report

1 reference

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7 July 2018

Molecular diagnosis of pituitary adenoma predisposition caused by aryl hydrocarbon receptor-interacting protein gene mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

Role of Brg1 and HDAC2 in GR trans-repression of the pituitary POMC gene and misexpression in Cushing disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

High prevalence of pituitary adenomas: a cross-sectional study in the province of Liege, Belgium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

Hereditary hormone excess: genes, molecular pathways, and syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

Cushing's disease in childhood as the first manifestation of multiple endocrine neoplasia syndrome type 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

A pleiomorphic GH pituitary adenoma from a Carney complex patient displays universal allelic loss at the protein kinase A regulatory subunit 1A (PRKARIA) locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

The prevalence of pituitary adenomas: a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

Pituitary disease in MEN type 1 (MEN1): data from the France-Belgium MEN1 multicenter study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

Pituitary macroadenoma in a 5-year-old: an early expression of multiple endocrine neoplasia type 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

Pituitary adenomas of the multiple endocrine neoplasia type I syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

7 July 2018

Sequence analysis of the PRKAR1A gene in sporadic somatotroph and other pituitary tumours

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01406.X

21 January 2018

Proliferation of transformed somatotroph cells related to low or absent expression of protein kinase a regulatory subunit 1A protein.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01406.X

21 January 2018

Somatic MEN1 gene mutation does not contribute significantly to sporadic pituitary tumorigenesis

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01406.X

21 January 2018

Pituitary adenoma predisposition caused by germline mutations in the AIP gene.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01406.X

21 January 2018

Aryl hydrocarbon receptor-interacting protein gene mutations in familial isolated pituitary adenomas: analysis in 73 families.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01406.X

21 January 2018

Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01406.X

21 January 2018

Multiple endocrine neoplasia type 1 variant with frequent prolactinoma and rare gastrinoma

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01406.X

21 January 2018

PRKAR1A, one of the Carney complex genes, and its locus (17q22-24) are rarely altered in pituitary tumours outside the Carney complex

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01406.X

21 January 2018

The role of the aryl hydrocarbon receptor-interacting protein gene in familial and sporadic pituitary adenomas.

1 reference

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21 January 2018

Aryl hydrocarbon receptor interacting protein variants in sporadic pituitary adenomas

1 reference

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21 January 2018

Prevalence of pituitary adenomas: a community-based, cross-sectional study in Banbury (Oxfordshire, UK).

1 reference

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26 October 2018

Nelson's syndrome associated with a somatic frame shift mutation in the glucocorticoid receptor gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3050035

26 October 2018

Aryl hydrocarbon receptor interacting protein(AIP) gene mutation analysis in children and adolescents with sporadic pituitary adenomas

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01406.X

21 January 2018

Germline inactivating mutations of the aryl hydrocarbon receptor-interacting protein gene in a large cohort of sporadic acromegaly: mutations are found in a subset of young patients with macroadenomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/20507346

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A kindred with a variant of multiple endocrine neoplasia type 1 demonstrating frequent expression of pituitary tumors but not linked to the multiple endocrine neoplasia type 1 locus at chromosome region 11q13

1 reference

https://pubmed.ncbi.nlm.nih.gov/20507346

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cushing's disease as the first clinical manifestation of multiple endocrine neoplasia type 1 (MEN1) associated with an R460X mutation of the MEN1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/20507346

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cushing's syndrome due to a pituitary corticotropinoma in a child with tuberous sclerosis: an association or a coincidence?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20507346

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The MEN-1 Gene Is Rarely Down-Regulated in Pituitary Adenomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/20507346

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

P53 gene mutation in an atypical corticotroph adenoma with Cushing's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/20507346

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1111/J.1399-0004.2010.01406.X

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Europe PubMed Central

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3 February 2020

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3 February 2020

PubMed publication ID

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3 February 2020

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